Understanding the process of formation of the complexes
between Spike protein variants that make up the structure of the SARS-CoV2
virus and human antibodies, brings light into how variations have an impact on
this complex formation. In this work, databases such as CoV3D, PDB and
pyDockWEB were used to collect sequencing results and structures of SARS-CoV2
variants. Finally, molecular docking was also used in order to predict the
interaction between the virus' Spike protein and antibodies. These results were
then made available on a website produced exclusively for public dissemination
of these analyses. Among other answers, this work serves as a guideline for
molecular docking studies of the interaction between Spike protein variants and
human antibodies.
Author(s) Details
Sérgio Amorim de
Alencar
Postgraduate Program in Genomic Sciences and Biotechnology,
Catholic University of Brasília, Brasília-DF, Brazil.
Rickson Passos Campoe
Postgraduate Program in Genomic Sciences and Biotechnology,
Catholic University of Brasília, Brasília-DF, Brazil.
Yasmin Rezende
Postgraduate Program in Genomic Sciences and Biotechnology,
Catholic University of Brasília, Brasília-DF, Brazil.
Rute Pereira de Souza
Postgraduate Program in Genomic Sciences and Biotechnology,
Catholic University of Brasília, Brasília-DF, Brazil.
Please see the link:- https://doi.org/10.9734/bpi/rpmab/v4/1106
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